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1-Hour OGTT Plasma Glucose as a Marker of Progressive Deterioration of Insulin Secretion and Action in Pregnant Women

Considering old GDM diagnostic criteria, alterations in insulin secretion and action are present in women with GDM as well as in women with one abnormal value (OAV) during OGTT. Our aim is to assess if changes in insulin action and secretion during pregnancy are related to 1-hour plasma glucose conc...

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Autores principales: Ghio, Alessandra, Seghieri, Giuseppe, Lencioni, Cristina, Anichini, Roberto, Bertolotto, Alessandra, De Bellis, Alessandra, Resi, Veronica, Lacaria, Emilia, Del Prato, Stefano, Di Cianni, Graziano
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3332183/
https://www.ncbi.nlm.nih.gov/pubmed/22567007
http://dx.doi.org/10.1155/2012/460509
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author Ghio, Alessandra
Seghieri, Giuseppe
Lencioni, Cristina
Anichini, Roberto
Bertolotto, Alessandra
De Bellis, Alessandra
Resi, Veronica
Lacaria, Emilia
Del Prato, Stefano
Di Cianni, Graziano
author_facet Ghio, Alessandra
Seghieri, Giuseppe
Lencioni, Cristina
Anichini, Roberto
Bertolotto, Alessandra
De Bellis, Alessandra
Resi, Veronica
Lacaria, Emilia
Del Prato, Stefano
Di Cianni, Graziano
author_sort Ghio, Alessandra
collection PubMed
description Considering old GDM diagnostic criteria, alterations in insulin secretion and action are present in women with GDM as well as in women with one abnormal value (OAV) during OGTT. Our aim is to assess if changes in insulin action and secretion during pregnancy are related to 1-hour plasma glucose concentration during OGTT. We evaluated 3 h/100 g OGTT in 4,053 pregnant women, dividing our population on the basis of 20 mg/dL increment of plasma glucose concentration at 1 h OGTT generating 5 groups (<120 mg/dL, n = 661; 120–139 mg/dL, n = 710; 140–159 mg/dL, n = 912; 160–179 mg/dL, n = 885; and ≥180 mg/dL, n = 996). We calculated incremental area under glucose (AUC(gluc)) and insulin curves (AUC(ins)), indexes of insulin secretion (HOMA-B), and insulin sensitivity (HOMA-R), AUC(ins)/AUC(gluc). AUC(gluc) and AUC(ins) progressively increased according to 1-hour plasma glucose concentrations (both P < 0.0001 for trend). HOMA-B progressively declined (P < 0.001), and HOMA-R progressively increased across the five groups. AUC(ins)/AUC(gluc) decreased in a linear manner across the 5 groups (P < 0.001). Analysing the groups with 1-hour value <180 mg/dL, defects in insulin secretion (HOMA-B: −29.7%) and sensitivity (HOMA-R: +15%) indexes were still apparent (all P < 0.001). Progressive increase in 1-hour OGTT is associated with deterioration of glucose tolerance and alterations in indexes of insulin action and secretion.
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spelling pubmed-33321832012-05-07 1-Hour OGTT Plasma Glucose as a Marker of Progressive Deterioration of Insulin Secretion and Action in Pregnant Women Ghio, Alessandra Seghieri, Giuseppe Lencioni, Cristina Anichini, Roberto Bertolotto, Alessandra De Bellis, Alessandra Resi, Veronica Lacaria, Emilia Del Prato, Stefano Di Cianni, Graziano Int J Endocrinol Clinical Study Considering old GDM diagnostic criteria, alterations in insulin secretion and action are present in women with GDM as well as in women with one abnormal value (OAV) during OGTT. Our aim is to assess if changes in insulin action and secretion during pregnancy are related to 1-hour plasma glucose concentration during OGTT. We evaluated 3 h/100 g OGTT in 4,053 pregnant women, dividing our population on the basis of 20 mg/dL increment of plasma glucose concentration at 1 h OGTT generating 5 groups (<120 mg/dL, n = 661; 120–139 mg/dL, n = 710; 140–159 mg/dL, n = 912; 160–179 mg/dL, n = 885; and ≥180 mg/dL, n = 996). We calculated incremental area under glucose (AUC(gluc)) and insulin curves (AUC(ins)), indexes of insulin secretion (HOMA-B), and insulin sensitivity (HOMA-R), AUC(ins)/AUC(gluc). AUC(gluc) and AUC(ins) progressively increased according to 1-hour plasma glucose concentrations (both P < 0.0001 for trend). HOMA-B progressively declined (P < 0.001), and HOMA-R progressively increased across the five groups. AUC(ins)/AUC(gluc) decreased in a linear manner across the 5 groups (P < 0.001). Analysing the groups with 1-hour value <180 mg/dL, defects in insulin secretion (HOMA-B: −29.7%) and sensitivity (HOMA-R: +15%) indexes were still apparent (all P < 0.001). Progressive increase in 1-hour OGTT is associated with deterioration of glucose tolerance and alterations in indexes of insulin action and secretion. Hindawi Publishing Corporation 2012 2012-04-10 /pmc/articles/PMC3332183/ /pubmed/22567007 http://dx.doi.org/10.1155/2012/460509 Text en Copyright © 2012 Alessandra Ghio et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Study
Ghio, Alessandra
Seghieri, Giuseppe
Lencioni, Cristina
Anichini, Roberto
Bertolotto, Alessandra
De Bellis, Alessandra
Resi, Veronica
Lacaria, Emilia
Del Prato, Stefano
Di Cianni, Graziano
1-Hour OGTT Plasma Glucose as a Marker of Progressive Deterioration of Insulin Secretion and Action in Pregnant Women
title 1-Hour OGTT Plasma Glucose as a Marker of Progressive Deterioration of Insulin Secretion and Action in Pregnant Women
title_full 1-Hour OGTT Plasma Glucose as a Marker of Progressive Deterioration of Insulin Secretion and Action in Pregnant Women
title_fullStr 1-Hour OGTT Plasma Glucose as a Marker of Progressive Deterioration of Insulin Secretion and Action in Pregnant Women
title_full_unstemmed 1-Hour OGTT Plasma Glucose as a Marker of Progressive Deterioration of Insulin Secretion and Action in Pregnant Women
title_short 1-Hour OGTT Plasma Glucose as a Marker of Progressive Deterioration of Insulin Secretion and Action in Pregnant Women
title_sort 1-hour ogtt plasma glucose as a marker of progressive deterioration of insulin secretion and action in pregnant women
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3332183/
https://www.ncbi.nlm.nih.gov/pubmed/22567007
http://dx.doi.org/10.1155/2012/460509
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